BI Sample 2 Lab Volume of Object

 

 

Volume of an Irregular Object

 

 

Introduction

 

Everything is made of matter. Matter has physical and chemical properties. Physical properties are observable, such as mass, volume, and density. Mass is a fundamental property of an object generally regarded as equivalent to the amount of matter in the object. Volume is the amount of space it takes up. Density is the thickness of it the formula for density is D=M/V. The purpose of this experiment was to find the mass, volume, and density of three different objects.

 

Hypothesis

 

Determining the volume of an irregularly shaped object can help in determining density.

 

Materials

 

The materials used included a rubber stopper, a rock, a shell, a 100mL graduated cylinder, water, electronic balance, paper, and pencil.

 

Methods:

 

Obtain rubber a stopper, a shell, and a rock. Estimate and record the mass and volume of the three objects. Weigh and record each object. Take the graduated cylinder and fill halfway with water and record the volume. Add one object and record the new volume. Subtract initial volume from final, and record. Repeat with the other three objects.

 

Results:

 

Object Estimated mass (g) Estimated volume (ml) Actual mass (g) Volume of H2O (ml) Volume of object + H2O (ml) Object’s Volume (ml) Density D=m/v

(g/ml)

Rubber Stopper 8g 65ml 8.3g 50ml 56ml 6ml 1.38g/ml
Shell 2g 55ml 3.1g 50ml 53ml 3ml 1g/ml
Rock 4g 60ml 7.8g 50ml 54ml 4ml 1.95g/ml

1. How did you determine the object’s:

a. Mass? Weighed it on a electronic balance

 

b. Volume? Put it in the water and measured the volume then subtracted the volume of the water before the object.

c. Density? Divided mass into volume

2. How did your estimates of mass and volume compare to the actual mass and volume of each object?

Our estimates of mass were close to the actual mass. Our estimates of volume were off not close to the actual volume at all.

3. Objects will sink if they are denser than water. Explain why ships made of steel float instead of sinking since steel is denser than water.

Because the ship has a hallow cavity with trapped air in it.

 

Error Analysis:

 

The volume of the water might not have been measured correctly.

 

Discussion and Conclusion:

 

The volume of the rubber stopper, rock and shell were determined by submerging them in a graduating cylinder containing water. The original water level in the cylinder was subtracted from the final water level to get the volume (ml) of each object. The actual mass (g) of each object was obtained by placing each on an electronic balance. Density could then be determined by dividing the mass of each object by its volume. The data showed the rock to have the greatest density at 1.95 g/ml with the rubber stopper 1.38 g/ml and the shell 1 g/ml being less dense.

BACK

 

Bi Sample Metric Measure

 

Metric Measurement Lab   

Introduction:

            Every scientific experiment in some way involves measurement.  Scientists worldwide use the metric system to display the results of measurements.  This system simplifies calculations based on a decimal system (powers of ten), opposed to the confusing English system of measurement.  Less confusion and better communication between scientists around the world makes the metric system more efficient than the English system for use in experiments.  The useful prefixes of the metric system are also known as the International System of Units (SI).

            Two measurements explored in this lab are mass and volume.  Mass is represented by grams, while volume is represented by milliliters (liquid) and cubic centimeters (solids with ruler measurement).  The purpose of this investigation is to get acquainted with and be accurate with the metric system.

Hypothesis:

By using a graduated cylinder, mass balance, and metric ruler, mass and volume can be found.  

Materials:

The materials used in this experiment include a graduated cylinder, an eyedropper, and a beaker of water for Part A; 20 ml of water, a graduated cylinder, and three marbles for Part B; a metric ruler, mass balance, three marbles, and a graduated cylinder for Part C; a metric ruler for Part D; and a graduated cylinder, eyedropper, six labeled test tubes, and three 25ml beakers of colored water (one with red, one with blue, and one with yellow) for Part E.  

Methods:

Part A:  Count you drops!

Fill a small graduated cylinder with 10 ml of water.  Count and record the number of drops it takes to raise the water to 11ml.  Leave the water in the graduated cylinder and count and record the number of drops it takes to raise the water to 12ml.  Leave the water in the graduated cylinder and count and record the number of drops it takes to raise the water to 13ml.  Calculate the average number of drops and round to the nearest tenth.

Part B:  Water Displacement

Add 20ml of water to a 100ml graduated cylinder.  Record this amount in the chart.  Add three marbles to the cylinder and measure and record the volume.  Find the difference between the two measurements and record it in the chart.  The difference between the two measurements will be the volume of the three marbles.

Part C:  Mass Mania

Check to see that the Pinter on the balance is pointing to zero.  If it is not, check to see that all the Riders (weights) are all the way to the left at the Zero mark.  Adjust the balance by turning the Adjustment Screw slowly until it points at zero.  Place the metric ruler on the pan and read and record the ruler’s mass.  After resetting the balance to zero, measure and record the mass of the empty 50ml graduated cylinder and then the three marbles.  Reset the balance to zero when all items have been massed. 

Part D:  Volume by Formula

Use the formula Volume=length x width x height to find the volume of the box.  Measure to the nearest centimeter before calculating the answer.  If necessary, round the answer to two decimal places.

Part E:  Color Challenge

Obtain the following items from the teacher:  3 beakers with colored water-25ml of each color (red, blue, and yellow), 1 graduated cylinder (25ml to 50ml), 1 eyedropper, and 6 test tubes labeled A, B, C, D, E, and F.  Perform each of the following steps using accurate measurements.  Measure 17ml of red water from the beaker and po9ur it into test tube A.  Measure 21ml of yellow water from the beaker and pour it into test tube C.  Measure 22ml of blue water from the beaker and pour it into test tube E.  Measure 5ml of water from test tube A and pour it into test tube B.  Measure 6ml of water from test tube C and pour it into test tube D.  Measure 8ml of water from test tube E and pour it into test tube F.  Measure 5ml of water from test tube C and pour it into test tube B.  Measure 2ml of water from test tube A and pour it into test tube F.  Measure 4ml of water from test tube E and pour it into test tube D.  Record the results in the chart.

Results:

Part A:  Count your drops!

# of drops to 11ml # of drops to 12ml # of drops to 13ml Average
24 26 25 25
  1. Take a guess—how many drops of water will it take to equal 1 milliliter?  18 drops.
  2. Based on your average, how close were you to your guess?  7 drops off of average.
  3. Based on your average, how many drops would it take to make 1 liter?  25,000 drops.

Part B:  Water Displacement

 

Volume of Water Before Adding Marbles (ml) Volume of Water After Adding Marbles (ml) Difference in Volume (ml) Volume of 3 marbles (ml)
20ml 25ml 5ml 5ml

 

Part C:  Mass Mania

 

Mass of Metric Ruler (g) Mass of Empty 50ml graduated cylinder (g) Mass of 3 Marbles (g)
3.0g 31.5g 11.0g

 

Part D:  Volume by Formula

Volume= length x width x height

7.0 cm x 1.0 cm x 3.0 cm = 21.0 cubic centimeters

Part E:  Color Challenge

 

Test Tube Color Final Volume (ml)
A Red 10ml
B Orange 10ml
C Yellow 10ml
D Green 10ml
E Blue 10ml
F Purple 10ml

 

 

Discussion and Conclusion:

By using a graduated cylinder, mass balance, and metric ruler, mass and volume can be found.  The purpose of Part A was to be accurate with reading graduated cylinders and how many drops of water make one milliliter.  This was accomplished by using an eyedropper to count the drops and reading the bottom of the meniscus to see when to stop dropping.  The average was found by adding the number of drops it took to reach the next milliliter (three times repeated) together and dividing by how many times the experiment was repeated which was three times.  (24+26+25)/3=25 average drops.  The purpose of Part B was to use water displacement to find volume.  In this particular experiment, water displacement was used to find the volume of three marbles.  To do this, the volume of the water before adding the marbles (20ml) was subtracted from the volume of the water after adding the marbles (25ml), to get the difference in the two volumes (5ml) which ultimately was the volume of the three marbles (5ml).  25ml-20ml=5ml.  The purpose of part C was to learn to use the balance accurately to determine the mass of an object(s).  To use a balance, the pointer and weights must be set at zero.  The mass of the three marbles, empty graduated cylinder, and metric ruler were found by placing them on the pan of the balance and moving the weights until the pointer was at zero again.  Mass is measured in grams.  The purpose of Part D was to use a metric ruler properly and apply your measurements to a formula to find volume.  To fill in the volume formula, length, width, and height of the box was found in the nearest centimeter with the metric ruler.  After those measurements were found, they had to be multiplied together to find the volume in cubic centimeters.  7cm x 1cm x 3cm=21 cubic cm.  Volume is expressed with cubic centimeter for solids and milliliters for liquids.  The purpose of Part e was to be accurate in liquid measurements to find the color and volume of the six test tubes.  This was accomplished by taking certain amounts of colored water from some beakers of test tubes and adding them to other test tubes.  If something was not measured right, the water in the test tube would not be the correct color.  It is important to always use accurate methods and measurements because details matter in science and experiments.

 

Bicalendar 2010-11 Revised

 

 

1st Semester Biology 2010-2011

 

 

AUGUST SEPTEMBER OCTOBER NOVEMBER DECEMBER JANUARY FEBRUARY MARCH APRIL MAY

 

THESE ARE APPROXIMATE DATES FOR ASSIGNMENTS!

 

2010

Monday Tuesday Wednesday Thursday Friday
16 17 18 19 20
 

23 24 25 26 27

 

 

30 31

 

 

TOP

 

2010

Monday Tuesday Wednesday Thursday Friday
1 2 3
TARGET PRE-TEST

6 7 8 9 10

 

13 14 15 16 17

 

20 21 22 23 24

INTERIMS
P-T Conference SHS

 

P-T Conference SJHS

 

27 28 29 30  

 

 

 

TOP

 

2010

Monday Tuesday Wednesday Thursday Friday
1
4 5 6 7 8

 

 

11 12 13 14 15

Professional Development
 

END OF FIRST 9 WEEKS

18 19 20 21 22

25 26 27 28 29
 

 

 

TOP

 

2010

Monday Tuesday Wednesday Thursday Friday
1 2 3 4 5
TARGET TEST #1 MC

8 9 10 11 12

 

15 16 17 18 19
22 23 24 25 26
 
29 30
 

 

TOP

 

2010

Monday Tuesday Wednesday Thursday Friday
1 2 3
SHS SCIENCE FAIR

 

6 7 8 9 10
TARGET TEST #2 EBR

 

13 14 15 16 17

Proficient-Advanced Students Out

TEST REVIEW
Proficient-Advanced Students Out
SEMESTER TEST
Proficient-Advanced Students Out
SEMESTER TEST
Proficient-Advanced Students
Out
 

SEMESTER TEST
Proficient-Advanced Students
Out
END OF 2ND 9 WEEKS

 

Enjoy Your Christmas Vacation December18, 2010 – January 4, 2011!

 

TOP

 

2nd Semester Biology

 

 

2011

Monday Tuesday Wednesday Thursday Friday
 3 4 5 6 7

10 11 12 13 14

17 18 19 20 21

MLK DAY!
24 25 26 27 28
31

 

 

 

TOP

 

2011

Monday Tuesday Wednesday Thursday Friday
1 2 3 4

P-T Conference SJHS

 

P-T Conference SHS

 

7 8 9 10 11
TARGET TEST #3 HE

14 15 16 17 18
President’s Day

 

21 22 23 24 25

  • Protist worksheet DUE
  • Continue Protist & Fungi PowerPoint

28

 

TOP

 

2011

Monday Tuesday Wednesday Thursday Friday
1 2 3 4

 

7 8 9 10 11

LITERACY TEST

LITERACY TEST

 

 

 

14 15 16 17 18

END OF 3RD 9 WEEKS

TARGET TEST #4 CDL

 

21 22 23 24 25
BREAK BREAK BREAK BREAK BREAK
28 29 30 31

 

TOP

 

2011

Monday Tuesday Wednesday Thursday Friday
1
4 5 6 7 8

 

11 12 13 14 15
  • TEST over Vertebrates
  • Handout: Notes on Plants and Plant Worksheet

  • Work on Plant Worksheet

  • Work on Plant Worksheet
  • Work on Plant Worksheet

 

  • Plant Worksheet DUE
18 19 20 21 22

 

EOC GEOMETRY

EOC GEOMETRY

25 26 27 28 29
EOC BIOLOGY
EOC BIOLOGY
  • Start Birds PowerPoint and answer worksheet questions

 

TOP

 

2011

Monday Tuesday Wednesday Thursday Friday
 2 3 4 5 6
  •  Continue Birds PowerPoint and answer worksheet questions

9 10 11 12 13

16 17 18 19 20
  • Teach wing spreading
  • Identify Insects (KEY)
  • Teach Card pointing
  • Identify Insects (KEY)
TARGET POST TEST

 

23 24 25 26 27

 

SEMESTER TEST
REVIEWBOOK RETURN
SEMESTER TEST
REVIEWBOOK RETURN
SEMESTER TEST
30 31
MEMORIAL DAY SEMESTER TEST

 

 

 

  2011

Monday Tuesday Wednesday Thursday Friday
1 2 3
    SEMESTER TEST

 MAKE UP EXAMS

TEACHERS LAST DAY

 

BACK

Ap Lab 1 Sample 5

 

Osmosis & Diffusion – Lab 1 

Introduction:

All molecules have kinetic energy and are constantly in motion.  This motion causes the molecules to bump into each other and move in different directions.  The result is diffusion.  Diffusion is the random movement of molecules from an area of high concentration to an area of low concentration. This will continue until dynamic equilibrium is reached; no net movement will occur.  Osmosis is a special kind of diffusion.  It is the diffusion of water through a selectively permeable membrane. A selectively permeable membrane means that the membrane will only allow certain molecules through such as water, small solutes, oxygen, carbon dioxide, and glucose, because no additional ATP is required. The membrane will not let ions, nonpolar molecules, or large molecules through because extra ATP is needed for them to travel across the membrane.  Active transport is how molecules (such as ions) move against the concentration gradient.  Additional ATP is required to perform this process.

Water will travel from an area of high water potential to an area of low water potential.  Water potential is the measure of free energy of water in a certain solution.  It is measured by using the Greek letter psi (ψ).  The formula for figuring water potential is:

ψ          =             ψp             +           ψs

Water Potential   =   Pressure Potential   +  Solute Potential

Water potential is affected by 2 different factors.  They are the addition of a solute and the pressure potential.  If a solute is added to the water, then the water potential is lowered.  If more pressure is placed on the water, then the potential is raised. The addition of a solute and water potential are inversely proportional.  Pressure being placed onto the water and the potential of the water are directly proportional.

Solutions can have three relationships with each other; isotonic, hypertonic, or hypotonic.  When the solutions have the same concentration of solutes, they are isotonic.  There is no net change in the amount of water on each side of the membrane.  If the solutions differ in their solute concentrations, the solution that has the most solute is hypertonic to the other solution.  The solution with the smaller amount of solute is hypotonic to the other solution. The net movement of water will be from the hypertonic solution to the hypotonic solution. Net movement will occur until dynamic equilibrium is reached, then there will be no net movement of water.

Hypothesis:

In this lab, osmosis and diffusion will occur between the solutions of different concentration until dynamic equilibrium is reached and there is no net movement of water.

Materials:

Exercise 1A:

The materials used include a 30cm piece of 2.5cm dialysis tubing, string, scissors, 15mL of 15% glucose/1% starch solution, 250mL beaker, distilled water, and 4mL of Lugol’s solution (Iodine Potassium-Iodine or IKI).

Exercise 1B:

This exercise required six 30cm strips of presoaked dialysis tuning, six 250mL cups or beakers, string, scissors, a balance, and 25mL of  these solutions: distilled water, 0.2M sucrose, 0.4M sucrose, 0.6M sucrose, 0.8M sucrose, and 1.0M sucrose.

Exercise 1C:

The materials that were required include 100mL of these solutions: distilled water, 0.2M sucrose, 0.4M sucrose, 0.6M sucrose, 0.8M sucrose, and 1.0M sucrose, six 250mL beakers or cups, a potato, a cork borer, a balance, paper towel, and plastic wrap.

Exercise 1D:

The materials used include a calculator, and a pencil.

Procedure:

Exercise 1A:

Soak the dialysis tubing in water.  Tie off one end of the tubing to form a bag.  Open the bag and place the glucose/starch solution in it.  Tie off the other end of the bag, leaving enough room for expansion of the contents in the bag.  Record the color of the solution in Table 1.1.  Next, test the glucose/starch solution for the presence of glucose.  Record the results in Table 1.1.  Fill a 250mL beaker or cup with 2/3 full with distilled water.  Add 4mL of Lugol’s solution to the distilled water and record the color of the solution in Table 1.1.  Test the solution for glucose and record the results in Table 1.1.  Immerse the bag in the beaker of solution.  Allow the beaker and bag to stand for approximately 30 minutes or until you see a distinct color change in the bag and the beaker.  Record the final color of the solution in the bag, and the solution in the beaker, in Table 1.1.  Test the liquid in the beaker and in the bag for the presence of glucose.  Record the results in Table 1.1.

Exercise 1B:

Obtain the six strips of presoaked dialysis tubing and create a bag out of each one by tying off one end.  Pour 25mL of the 6 solutions into separate bags. Tie off the other end of the 6 bags.  Rinse each bag gently with distilled water and blot dry.  Determine the mass of each bag and record it in Table 1.2.  Immerse each bag in one beaker filled will distilled water and label the beaker to indicate the molarity of the solution in the bag.  Let the setups stand for 30 minutes.  Remove the bags from the water.  Carefully blot them dry and determine their masses.  Record them in Table 1.2.  Obtain the other lab groups data to complete Table 1.3.

Exercise 1C:

Pour 100mL of the solutions into a labeled 250mL beaker.  Use a cork borer to cut potato cylinders.  You need 4 cylinders for each cup.  Determine the mass of the 4 cylinders together and record the amount in Table 1.4.  Place the cylinders into the beaker of sucrose solution.  Cover the beaker with plastic wrap to prevent evaporation.  Let it stand overnight.  Remove the cores from the beaker and blot them gently on a paper towel and determine their total mass.  Record the results in Table 1.4.  Calculate the percentage change.  Do this for the individual and class data.  Graph the class average percentage change in mass.

Exercise 1D:

Determine the solute, pressure, and water potential of the sucrose solution.  Then, graph the information that is given about the zucchini cores.

Results:

Exercise 1A:

 Table 1.1

 

Initial Contents Initial Color Final Color Initial Presence of Glucose Final Presence of Glucose
Bag 15% glucose & 1% starch Cloudy White Purple Yes Yes
Beaker Water & IKI Brown Orange No Yes

 

  1. Which substances are entering the bag and which are leaving the bag? What evidence supports the answer?  Distilled water and IKI are  leaving and entering.  Glucose is able to leave the bag.
  2. Explain the results that were obtained.  Include the concentration differences and membrane pore size in the discussion.  Glucose and small molecules were able to move through the pores.  Water and IKI moved from high to low concentration.
  3. How could this experiment be modified so that quantitative data could be collected to show that water diffused into the dialysis bag?  You could mass the bag before and after it was placed into the solution.
  4. Based on your observations, rank the following by relative size, beginning with the smallest: glucose molecules, water molecules, IKI molecules, membrane pores, and starch molecules.  Water molecules, IKI molecules, Glucose molecules, Membrane pores, and Starch molecules
  5. What results would you expect if the experiment started with a glucose and IKI solution inside the bag and only starch and water outside?  The glucose and IKI would move out of the bag and turn the starch and water solution purple/blue.  The starch couldn’t move inside the bag because its molecules are too big to pass through the membrane of the tubing.

Exercise 1B:

 

Table 1.2: Dialysis Bag Results: Individual Data

 

Contents in dialysis bag Initial mass (g) Final mass (g) Mass difference (g) % Change in mass
Distilled Water 24.7 23.7 1 4.1
0.2M 26.7 27.4 .7 2.62
0.4M 27.4 29 1.6 5.84
0.6M 25.9 29 3.1 12
0.8M 29 32.6 3.6 12.41
1.0M 28 33.7 5.7 20.4

 

Table 1.3: Dialysis Bag Results: Class Data

 

Group 1

Group 2

Group 3

Total Class Average
Distilled Water 4.1% .7% 1.6% 6.4% 2.13%
0.2M 2.62% 6.4% 4.1% 13.12% 4.37%
0.4M 5.84% 9.9% 9.5% 25.24% 8.41%
0.6M 12% 13.4% 9.3% 34.37% 11.57%
0.8M 12.41% 14.6% 15.2% 42.21% 14.07%
1.0M 20.4% 19.7% 15.9% 56% 18.67%

 

  1. Explain the relationship between the change in mass and the molarity of sucrose within the dialysis bags.  The solute is hypertonic and water will move into the bag.  As the molarity increases the water moves into the bag.
  2. Predict what would happen to the mass of each bag in this experiment if all the bags were placed in a 0.4M sucrose solution instead of distilled water.  Explain.  With the 0.2M bag, the water would move out.  With the 0.4M bag, there will be no net movement of water because the solutions reach dynamic equilibrium.  With the 0.6M-1M bags, the water would move into the bag.
  3. Why did you calculate the percent change in mass rather than simply using the change in mass?  This was calculated because each group began with different initial masses and we would have different data.  All the groups needed consistent data.
  4. A dialysis bag is filled with distilled water and then places in a sucrose solution.  The bag’s initial mass is 20g and its final mass is 18g.  Calculate the percent change of mass, showing your calculations.  ((18-20)/20) x 100 = 10%
  5. The sucrose solution in the beaker would have been hypotonic to the distilled water in the bag.

Exercise 1C

 

Table 1.4: Potato Core: Individual Data

 

Contents of Beaker Initial Mass (g) Final Mass (g) Difference in Mass % Change in Mass
Distilled Water 2.8 3.7 .9 32.14
0.2M 2.9 3.1 .2 7
0.4M 2.5 2.2 .3 12
0.6M 2.3 1.9 .4 17.39
0.8M 2.5 1.9 .6 24
1.0M 2.3 1.8 .5 21.74

 

Table 1.5: Potato Core: Class Data

 

Group 1 Group 2 Total Class Average
Distilled Water 32.14% 21.1% 53.24% 26.62%
0.2M 7% 6.7% 13.7% 6.85%
0.4M -12% -6.5% -18.5% -9.25%
0.6M -17.39% -15.2% -32.59% -16.30%
0.8M -24% -20% -44% -22%
1.0M -21.74% -19% -40.74% -20.37%

 

Determine the molar concentration of the potato core.  0.3M

Exercise 1D

 

 

What is the molar concentration of the zucchini cores? .35M

 

  1. If a potato core is allowed to dehydrate by sitting in the open air, would the water potential of the potato cells decrease or increase? Why?  It would decrease because the water would leave the cells and cause the water potential to go down.
  2. If a plant cell has a lower water potential than its surrounding environment and if pressure is equal to zero, is the cell hypertonic or hypotonic to its environment? Will the cell gain water or lose water?  It is hypotonic and it will gain water.
  3. The beaker is open to the atmosphere.  What is the pressure potential of the system?  The pressure potential is zero.
  4. Where is the greatest water potential?  In the dialysis bag.
  5. Water will diffuse out of the bag. Why? It is because the water moves from and area of high water potential to an area of lower water potential.
  6. What effect does adding solute have on the solute potential component of that solution? Why?  It makes is more negative.
  7. Consider what would happen to a red blood cell placed in distilled water: a) Which would have the higher concentration of water molecules?  Distilled Water  b) Which would have the higher water potential?  Distilled Water  c)  What would happen to the red blood cell? Why?  It would lyce, because it would take on too much water.

Error Analysis:

Possible errors that could have affected the results of the lab include incorrectly mixing the solutions, ineffectively tying the dialysis tubing, inaccurately measuring , and inaccurately calculating.

Conclusion:

            During Exercise 1A the data that was collected help determine which molecules can and can not move across a cell membrane. Obviously, because of the color change in the bag, the IKI was able to move across the membrane.  It is small enough to fit through the pores in the selectively permeable membrane, along with water.  Starch was too large to move across the membrane. Glucose, as the Benedict’s test proves, was able to move freely along with the water and IKI solution.

In Exercise 1B, it was proven that water moves faster across the cell membrane than sucrose.  The water moved to help reach dynamic equilibrium between the 2 solutions.  The sucrose molecules are too big to move across the membrane as fast as water can.

The data in Exercise 1C showed that the potatoes contained sucrose.  The sucrose in the potato raised the solute potential, which lowered the water potential.  The beaker of distilled water had a high water potential.  Water moves down the concentration gradient, causing the potato cores to take on water.

Exercise 1D helped better understand the lab with simple algebra equations.  It proved that the data that was collected was correct through mathematics.

 

AP Biology Powerpoints 8th ed

 

 

 

AP Biology PowerPoints

Chapter 1 Introduction Chapter 20 Biotechnology Chapter 39 Plant Responses
Chapter 2 Biochemistry Chapter 21 Genomes Chapter 40 Animal Form & Structure
Chapter 3 Water Chapter 22 Darwin Evolution Chapter 41 Animal Nutrition
Chapter 4 Carbon Chemistry Chapter 23 Population Evolution Chapter 42 Circulation & Respiration
Chapter 5 Macromolecules Chapter 24 Origin of Species Chapter 43 Immune System
Chapter 6 The Cell Chapter 25 Earth History Chapter 44 Osmoregulation
Chapter 7 Cell Membranes Chapter 26 Phylogeny Chapter 45 Endocrine System
Chapter 8 Metabolism Chapter 27 Archea & Bacteria Chapter 46 Animal Reproduction
Chapter 9 Cellular Respiration Chapter 28 Protists Chapter 47 Animal Development
Chapter 10 Photosynthesis Chapter 29 Plant Diversity I Chapter 48 Neurons
Chapter 11 Cell Communication Chapter 30 Plant Diversity II Chapter 49 Nervous System
Chapter 12 Cell Cycle Chapter 31 Fungi Chapter 50 Senses
Chapter 13 Meiosis Chapter 32 Introduction to Animals  Chapter 51 Behavior
Chapter 14 Mendel Chapter 33 Invertebrates Chapter 52 Ecology
Chapter 15 Chromosomes Chapter 34 Vertebrates Chapter 53 Population Ecology
Chapter 16 Molecular Inheritance Chapter 35 Plant Structure Chapter 54 Community Ecology
Chapter 17 From Gene to Protein Chapter 36 Transport in Plants Chapter 55 Ecosystems
Chapter 18 Gene Expression Chapter 37 Plant Nutrition Chapter 56 Conservation
Chapter 19 Viruses Chapter 38 Angiosperms